TIC BOPYRID ISOPODS OF THE AMPHI-AMERICAN GENUS OPHRYXUS THOMPSON WITH THE DESCRIPTION OF A NEW SPECIES FROM CALIFORNIA JOHN C.

f zc OOLOGY UBRPm O'fyk/^/fc'Jtf/??, J TIC BOPYRID ISOPODS OF THE AMPHI-AMERICAN GENUS OPHRYXUS THOMPSON WITH THE DESCRIPTION OF A NEW SPECIES FROM CALIFORNIA JOHN C. MARKHAM 1 ABSTRACT: Stegophryxus hyptius. heretofore known only as a parasite of Pagurus lomiiccirpus in New England, is recorded infesting P. longicarpus in Georgia. P. annulipes in North Carolina and Georgia, and P. bonairensis and P. miamensis in southern Florida. The only known specimens of Stegophryxus thompsoni. the types, from an unknown host in Chile, are redescribed. A new species from California and Baja California. S. hyphalus, is described as a parasite of Parapagurodes laurentae and P. makarovi. These three species, the only members of the genus, are illustrated in detail and their distribution discussed.,- xafll ination of shallow-water hermit crabs collated along the Atlantic coast from Florida to \orth Carolina has turned up several specimens lt the athelgine bopyrid parasite Stegophryxus livptius Thompson, previously known only from New England, thereby providing several new host records and a considerable extension of range for this species. Reexamination of the types of S. thompsoni Nierstrasz and Brender a Brandis from Chile, which had not been adequately described, became possible. Numerous parasites of hermit crabs taken off the coast of California and Baja California proved to belong to a new species. With these three species of Stegophryxus described, it became possible to review the genus in detail. The material examined was in or has been donated to the following museums: Allan Hancock Foundation, University of Southern California (AHF); Rijksmuseum van Natuurlijke Historic Leiden (RMNHL); Rosenstiel School of Marine and Atmospheric Science, University of Miami (UMML); United States National Museum of Natural History, Smithsonian Institution (USNM); and Universitetets Zoologiske Museum, Copenhagen (ZMC). Stegophryxus Thompson 1902 Type-species, by original designation, hyptius Thompson. Stegophryxus hyptius Thompson 1902 Figures 1-3 Stegophryxus Sumner et ah, 1913a, p. 136; 1913b, p. 661. Kunkel, 1918, p. 236. Reinhard et al.. 1947. pp. 70-72. Reinhard, 1949, pp. 17-31: 1956. p. 101. Reinhard and Buckeridge, 1950, p. 131. Caullery. 1950, p. 97; 1952, p. 76. Reverberi, 1952, p. 292. von Brand, 1952, pp. 256. 271. tab. 41; 1966. p. 222, tab. 38. Florkin, 1960, p. 405. Noble and Noble, 1964, pp. 392, 393, figs. XVI-5A, 5B, 5C Smith, 1964, p. 105. Kaestner, 1970, p. 463. Bourdon, 1968, p. 133. Schultz. 1969, pp. 321 322, fig. 513. Markham, 1972, p. 73. Stegophryxus hyptius. Miner, 1950, pp. 450. 453. pi. 145. Stegophrixus hyptius. Nierstrasz and Brender a Brandis, 1931, pp. 197-198. Stegophryxus. Baffoni, 1953, p. 447. Reinhard. 1956, p. 93. Kaestner. 1967, p. 1161: 1970. pp. 425, 463. Material examined. Infesting Pagurus bonairensis Schmitt. Bear Cut, Virginia Key, Miami, Florida, 9 February 1958, A. J. Provenzano, coll., 19, 1, USNM 101762. In Thalassia bed, shallow water, NW side Virginia Key, Miami, Florida, 25 March 1969. J. C. Markham, coll., 19. 1 6 (reference 6 ), USNM. Same locality, 8 November 1972, E. B. Hatfield, coll.. 19, lcj, AHF. Same locality. 12 February 1973, E. B. Hatfield, coll., 19 (reference 9), Id, USNM. Shallow subtidal, off W. Arsenicker Key, Card Sound, Florida, 25 October 1972, E. B. Hatfield, coll.. 19, IS, UMML 32.4538. Infesting Pagurus miamensis Provenzano. In Thalassia bed, shallow water, NW side Virginia Key, Miami, Florida, 28 June 1972, E. B. Hatfield, coll.. P. A. McLaughlin, identification of host, 19, 1 S. UMML 32.4539. Infesting Pagurus longicarpus Say. Tidepool, Sapelo Stegophryxus hyptius Thompson, 1902, pp. 53-56, pis. 9, 10. Richardson, 1904, pp. 59-60; 1905, pp. 532-535, figs. 578, 579. Rathbun, 1905, p. 48. 33 1 Rosenstiel School of Marine and Atmospheric Science, Univ. Miami, 10 Rickenbacker Causeway, Miami, Florida 33149.

34 BULLETIN SOUTHERN CA ACADEMY OF SCIENCES VOLVMP Figure 1. Stegophryxus hyptius Thompson, reference female. A. Dorsal view. B. Ventral view. C. Left antenna 2. D. Right posterior ventral border of head. E. Right oostegite 1, interior. F. Same, exterior. G. Right pereopod 1. H. Left pereopod 7. I. Pleon, dorsal view. Scale indicates 1.0mm for A, B, 0.5mm for D-F, I, 0.2mm for C, G, H. Beach, Georgia, August 1969. R. W. Heard, coll., one. immature 9, 1 3. USNM. Woods Hole, Massachusetts, date and coll. unknown, M. J. Rathbun, identification of host, 19, 1 <5, USNM 54777. Infesting Pagurus annulipes Stimpson, all hosts identified by P. A. McLaughlin. Morehead Channel, North Carolina, 3 March 1967, R. W. Heard, coll., 3 9, 3 i, four cryptoniscan larvae, ZMC. Same locality. 25 June 1970, R. W. Heard, coll., 49, 43, Figure 2. Stegophryxus hyptius Thompson, A-G, reference male. H. Second male. A. Dorsal view. B. Lateral view. C. Ventral view. D. Right antenna 2. E. Left antenna 1. F. Right pereopod 1. G. Left pereopod 7. H. Pleon and last pereomere, dorsal view. Scale at B, indicates 0.2mm for A-C, 0.1mm for D-G; scale at H. indicates 0.1 mm for H. Figure 3. Stegophryxus hyptius Thompson. A. \ m mature female, ventral view. B-F, cryptoniscan larva B. Dorsal view. C. Ventral view. D. Left antennae E. Left pereopod 1. F. Left pereopod 7. Scale i n. dicates 1.0mm for A, 0.1mm for B. C, 0.05mm f 0r D-F. two cryptoniscan larvae, RMNHL. Lacking collection data (probably North Carolina), 19, UMML i 32.4540. Beaufort, North Carolina, 1969 or 1970, C. Kellogg, coll., 19, 1(5, AHF. Same. 19. 1 &. both damaged, UMML 32.4541. Bulkhead Channel. Beaufort Harbor, North Carolina, 22 June 1970. C. Kellogg, coll., 19, 1 (5, AHF. Same, 19, 1 6. UMML 32.4542. Beaufort Harbor, North Carolina. 1969 or 1970, C. Kellogg, coll., 1 damaged 9. AHF. Remarks. Thompson (1902) presented a de- I tailed description and excellent drawings of both sexes, an immature female and a cryptoniscan larva of Stegophryxus hyptius. Richardson (1905) reproduced Thompson's descriptions and draw- : ings of the adults. There is thus no need to redescribe this species in detail, and a diagnosis should suffice. For comparison, I have presented drawings of both sexes collected in Florida (Figs. 1, 2), an immature female from Georgia (Fig. 3A) and more detailed drawings of a cryptoniscan from North Carolina (Figs. 3B-F). The characters which distinguish the females of S. hyptius (Fig. 1) are a head twice its width, a first oostegite which is bluntly pointed, a highly asymmetrical brood pouch which extends far back on the right side, a pleon which is less than half the total body length and bears very narrow lateral plates and pleopodal rami and enlarged prominent uropods. Males of S. hyptius (Fig. 2) are distinctive in having conspicuous eyes, the head clearly

BOPYRID PARASITES AND NE rated from the pereon, and the pleon markedly ovver than the last pereomere, roughly triangun ' nj ending in a rounded point. The immature 1,1,ip of S. hyptius can be distinguished by its,, 0f coxal plates, its elongate pleomeres and ' v prominent uropods. ^Tvvo of the host Pagnrus annulipes, in addition bearing mature pairs of Stegophryxus hyptius S the abdomen, also bore cryptoniscan larvae on thorax. On one P. annulipes there were two ptoniscans, one attached to the carapace, the * her to a pereopod; on the other P. annulipes, hree cryptoniscans were clinging to the carapace j a fourth was inside the branchial chamber. rhese larvae, one of which is pictured (Figs. ;8-F). agree in all respects with those which Thompson (1902) described, even though he tound them with the male in the brood chamber,f the female Stegophryxus rather than on the ^st's body. I have sent some of these larvae to j ar i-ove Stromberg of the University of Lund, who plans to examine them with a scanning electron microscope. One pair of Stegophryxus hyptius from Pagurus bonairensis was examined while still alive. The female was clinging so tightly to its host's pleopods that one pleopod was torn off in removing the parasite. Its only movement was a constant beating of the anterior oostegites to aerate the larvae filling the closed brood pouch. The male, rather than being in the female's brood pouch, as is tvpical, was crawling all over its body. The color of the female was transparent to whitish except that dorsally the gut was red-orange and the ovaries yellowish with developing eggs, and there were a few chalky white chromatophores scattered along the sides. The male was transparent except for black eyespots, a brownish gut and a network of interconnecting white lines in all pereomeres and the posterior third of the pleon. A second pair was examined freshly preserved. The female had a uniform glossy white background with brickred eyes, a pale yellow central dorsal region on the pereon and a few chalky white chromatophores scattered near the edges of the pereon; developing embryos visible through the oostegites bore rows of punctate red chromatophores. The accompanying male was also glossy white with black eyespots, an orange, gut and scattered black and white chromatophores. Previous records of S. hyptius are only from Rhode Island and Woods Hole, Massachusetts. At the latter locality it is so common that Reinhard (1949) used it in a classical study to demonstrate SPECIES FROM CALIFORNIA 35 sex determination in the Bopyridae, and Reinhard et al., (1947) made important discoveries about the effects it had on its host, which was always Pagurus longicarpus. The new records thus add a considerable extension of range, down to southern Florida, and several new host records, all species of Pagurus. Of the parasites examined, 17 were still with their hosts. Five of these hosts were males, 12 females, the females being hosts significantly more often. Stegophryxus thompsoni Nierstrasz and Brender a Brandis 1931 Figures 4-5 Stegophrixus thompsoni Nierstrasz and Brender a Brandis, 1931, pp. 196-198, figs. 87-89. Material examined. From unknown hermit crab. Valparaiso, Chile, exact locality and date unknown. Th. Mortensen Pacific Expedition, coll. Hoiotype 9, allotype, both damaged, ZMC. Redescription of holotypic female (Fig. 4). Body length 8.0mm, maximal body width 3.7mm, head length 1.6mm, pleon length 3.8mm, distortion of body axis 50 degrees. Body badly damaged, so outline uncertain (Fig. 4A). Head twice as long as wide. Segmentation of antenna 1 uncertain, antenna 2 (Fig. 4B) of five Figure 4. Stegophryxus thompsoni Nierstrasz and Brender a Brandis, hoiotype female. A. Dorsal view. B. Right antenna 2. C. Right maxilliped. D. Right posterior ventral border of head. E. Right oostegite 1, interior. F. Same, exterior. G. Left pereopod 2. H. Right pereopod 6. I. Pleon, ventral view. Scale indicates 1.0mm for A, C, E, F, I, 0.4mm for B, 0.25mm for D, 0.5mm for G. H.

36 BULLETIN SOUTHERN CALIFORNIA ACADEMY OF SCIENCES VOLUME 7 fl Redescription of allotypic male ^ig. 5). b 0d. length 2.3mm, maximal body width 0.8mm. hea 0 J length 0.3mm. pleon length 0.6mm. Sides of bon, nearly parallel, all segments clearly separated (Fj, 5A, B). Head semicircular, narrower than pereon. ^ eyes. Antennae (Figs. 5C, D) of three and five se e. ments. respectively. Pereon broadest, but only slightly so, across fou^ pereomere. All pereomeres separated by slight antern lateral indentations. Pereopods (Figs. 5E. F) gradh ally smaller posteriorly. Pleon nearly as broad as last pereomere, bareh longer than wide, broadly oval in outline, greater l width about : \ of distance back from anterior edg e No indication of segmentation. The male has broken into two pieces between th e third and fourth pereomeres. and one side of th e pleon is damaged, so the drawings presented are partial reconstructions. Stegophryxus hyphalus, new species Figures 6-8 Figure 5. Stegophryxus thompsoni Nierstrasz and Brender a Brandis, allotype male. A. Dorsal view. B. Ventral view. C. Left antenna 1. D. Left antenna 2. E. Right pereopod 1. F. Right pereopod 7. Scale indicates 1.0mm for A, B, 0.2mm for C-F. segments. No eyes. Maxilliped (Fig. 4C) with very irregular outline. Posterior ventral border of head (Fig. 4D) with long pointed lateral projection, irregular blunt process medial to it. Pereon surrounding head, first two pereomeres obliterated centrally, first five surrounding head, sixth longest. First oostegites (Figs. 4E, F) rounded anteriorly, with dentate internal ridge, sharply angled falcate posterolateral point. Most of other oostegites damaged or missing, so size, shape and position unknown. First five pereopods with prominent coxal plates, sharply re flexed, reduced in size (Fig. 4G): last two pereopods lacking coxal plates, more or less straight, larger (Fig. 4H). Last two pereomeres (Fig. 41) with medial ventral tubercles near anterior margins. Pleon nearly as long as pereon. gradually tapering posteriorly, of six pleomeres. Lateral plates and pleopodal rami (Fig. 41) all about the same size, ovate in outline: evidently pleopods and lateral plates lost from fourth and fifth pleomeres by damage. Uropods uniramous, oval, each nearly as large as whole last pleomere, extending far posteriorly from that pleomere. Tiny posterior point between uropods. IStegopliryxus sp. Menzies and Miller. 1954, pp 141, 153. Stegophryxus n. sp. McLaughlin and Haig. 1973, pp. 119, 134-135. Material examined. Infesting Parapagurodes lau. rentae McLaughlin and Haig (part of type seriesi collected by Allan Hancock Foundation Velero III among Santa Barbara Islands, California, and near Abrejos Pt., Baja California. Sta. 914-39, 32 47'N. 118 22'W, 143-319m, 19 February 1939, 1$, 1;. AHF; Sta. 981-39, 33 35'-35 08'N, 119 0r\V, 139-159m, 29 May 1939, 1$, U, AHF; Sta. 1012-39,, 32 46'N, 118 25'W, 100-126m, 9 November 1939.' one immature 5, AHF; Sta. 1028-39, 33 18'N, 118 : 16'W, 152-229m, 10 December 1939, 19, 1 6. ZMC: Sta. 1239-41, 33 01'N, 118 33'W, 95-112m, 11' February 1941, 1$, AHF; Sta. 1429-41, 33 17'N. 118 16'W. 159-174m, 25 October 1941, 59, U. AHF; Sta. 1710-49, 26 17'N, 113 41'W, 99m. 7 March 1949, one immature 9. USNM: Sta. 1937-50. 34 02'N, 119 27'W, 69-79m. 24 March 1950. one immature 9, ZMC. Infesting Parapagurodes makarovi McLaughlin and Haig (part of type series) collected by U.S. Bureau of Fisheries Steamer Albatross. Sta. 2946, in Santa Barbara Islands, California, 33 58'N, 119 0 31'W. 274m, 7 February 1889. 19, USNM. Sta. 3184, off Carmel, California, 36 27'N. 122 00'W, 141m,? April 1890, 19, lo', USNM. Collected by Velero III among Santa Barbara Islands, California, and near San Benito Islands, Baja California. Sta. 911-39. 39 00'N, 118 33'W, 110-155m, 18 February 1939. 19, 1<J. AHF; Sta. 981-39. 33 35'N, 119 8 01'W 139-159m, 29 May 1939, 7 9 (including one imma"^ ture). 36. AHF; Sta. 983-39, 33 44'N, 119 10'W v 3<M7./

Figure 6. Stegophryxus hyphalus, new species, holotype female. A. Dorsal view. B. Ventral view. C. Left antennae. D. Posterior ventral border of head. E. Right oostegite 1, exterior. F. Same, interior. G. Left pereopod 1. H. Left pereopod 6. Scale indicates 2.0mm for A, B, E. F, 1.0mm for D, 0.5mm for C, G, H. > v /- J > ^0(0" "?./. 3<*-!3o.l. x'io^jpc'. W~i1Ct."j, parormoe. -. 3=H3<0. 128m, 29 May 1939, 1$, AHF/sta. 1018-39, 33 (length 6.1mm, maximal body width 3.2mm, head Ol'N, 118 32"W, 110-247m, 23 November 1939, one 5 length 1.2mm, pleon length 2.3mm, distortion of body immature 2, RMNHL/Sta. 1020-39, 33 03'N, 118 5 axis 42 degrees. Body nearly oval in outline (Figs. 40'W, 247-274m, 24 November 1939, 22, 1 $, AHF;^!6A, B). Sta. 1026-39, 33 00'N, 118 38'W, 216-384m, 9 De-_^J Head roughly cordate in shape, about 1.5 times as cember 1939, holotype 2, AHF 3928, allotype $, $"long as broad. Antennae 1 and 2 (Fig. 6C) of 3 and AHF 3928a, two other 2, one other $, AHF;/Sta. $5 segments, respectively; each segment smaller than 1119-40, 28 13'N, 115 34'W, 159-174m, 19 Feb- $ that proximal to it. No eyes. Posterior ventral ruary 1940, 12. UMML 32.4543;/sta. 1173-40, 33 ^ border of head (Fig. 6D) with raised central portion 17'N, 118 14'W, 197-20lm, 20 August 1940, 12,^ consisting of a blunt medial point and two laterally AHF;/Sta. 1393-41, 33 47'N, 119 59'W, 196-229m, directed narrow rounded points; each side bearing a 26 August 1941, 12, 1<$, RMNHLy^ Collected by long tapering point laterally with irregularly shaped Velero IV near Santa Barbara Island, Sta. 2062-51, blunt projection medial to it. 33 33'N-34 33'N, 119 04'W, 256-296m, 18 October Pereon longer than broad. First five pereomeres 1951, 12, 16, UMML 32.4544. concave anteriorly, more or less concentrically sur- Description of holotypic female (Fig. 6). Body rounding head; first two pereomeres incomplete in

38 BULLETIN SOUTHERN CALIFORNIA ACADEMY OF SCIENCES VOLUMA Figure 7. Stegophryxus hyphalus, new species, immature female. A. Dorsal view. B. Ventral view. 1.0mm indicated. center; last two pereomeres concave posteriorly, narrower than others; sixth pereomere by far the longest. First oostegites (Figs. 6E, F) rounded anteriorly, without conspicuous internal ridge in circular middle region, produced into broadly falcate posterolateral point; first two pairs of oostegites arching over head; fifth oostegites by far the largest, covering half of ventral surface, both produced into posterolateral pockets of equal length, posterolateral borders lined with several long setae. Pereopods of first five pairs (Fig. 6G) surrounding head, sharply reflexed; last two pereopods (Fig. 6H) far posterior, longer and straighter than others. Pleon about % as long as pereon, of six pleomeres. Numerous tubercles on ventral surface of first two pleomeres. Sides of pleomeres 1-5 produced into foliaceous lanceolate lateral plates identical to branches of biramous pleopods. Final pleomere bearing small bulbous uniramous uropods. Variations: Some of the other females examined show a few slight variations from the type. In several cases, the uropods are somewhat longer; in others, the tubercles on the first two pleomeres are either longer and flatter or absent. Ten of the 33 females examined are immature to varying degrees, so remarks on their development are possible. At first, the body is nearly symmetrical, the small oostegites of equal size in each pair, gradually larger from the first to the fifth; the pleon, which is as long as the pereon and not abruptly narrower than it, extends straight back. In the earliest postlarval stages, only the exopodites of the pleopods are developed, the endopodites being small flaps and the lateral plates suggested by tiny bumps. As development progresses (Fig. 7), the branches of the pleopods become equal, while the corresponding lateral plates are still smaller. Other conspicuous differences of the immature females from adult ones are large coxal plates at the bases of all pereopods and much larger uropods. Description of allotypic male {Figs. 8A-E) length 2.6mm, maximal width 0.6mm, pleon W 0.7mm. Sides of pereon nearly parallel, head pleon abruptly narrower (Figs. 8A, B). Head much wider than long, fused with R pereomere. Antennae 1 and 2 (Fig. 8C) of three a, seven segments respectively, both bearing many ^ on distal segments. No eyes. Pereon broadest, but only slightly so, across sei and third pereomeres. All pereomeres separated lateral incisions. Pereopods (Figs. 8D. E) all of sj sa^, size, dactyli progressively smaller and carpi 1^ posteriorly. Pleon about Vt length of body, tapering to bin* point. No segments, but undulating margins j^ eating traces of segments. Appendages lack Ventral surface (Fig. 8F) bearing tiny paired slit j markings. Variations: Several males have their heads dk tinctly separated from their pereons, while the pleo* of some are quite wide relative to pereonal width In some cases (Fig. 8G) both of these variation occur. Etymology. The specific name hyphalus is the Latinized form of a Greek word meaning "sub. merged" in reference to the consistent occurrence of this species in much deeper water than S. hyptim Remarks. Stegophryxus hyphalus differs from the other two species of the genus in several respects. The female is similar to that of S. hyptius, from which it differs in lacking eyes at all stages, having a much more symmetrical brood pouch, smaller uropods in the adult, more prominent pereopodal coxal plates, shorter pleomeres, and smaller pleonal lateral plates in immature forms. The adult female of S. hyphalus differs from that' of S. thompsoni in having a relatively shorter head and pleon, more broadly pointed firf oostegites, less conspicuous pereopodal coxat plates, narrower pleonal lateral plates and pleo^ podal rami, and much smaller uropods. Males of; S. hyphalus differ from those of S. hyptius in lacking eyes, having pereomeres more strongly separated, and pleon longer, more pointed, and with more undulate margins. The male of S. hyphalus may be distinguished from that of 5. thompsoni by its shorter head and pointed pleon. It is entirely possible that all three species hav* eyes in both sexes; eyes have been observed only in live or freshly preserved specimens of S. hyptius. The only previous record of a Stegophryxus from the coast of California is that listed by Menzies and Miller (1954), who identified the host as a "Pagurus sp." Their key to species indicates that they did indeed have a Stegophryxus', most likely S. hyphalus. Unfortunately, they list no locality or source for this record.

I<)7< BOPYRID PARASITES AND NEW SPECIES FROM CALIFORNIA 39 A B Figure 8. Stegophryxus hyphalus, new species. A-E, allotype male. G, second male. A. Dorsal view. B. Ventral view. C. Right antennae. D. Right pereopod 2. E. Right pereopod 7. F. Pleon, ventral view. G. Dorsal view. Scale indicates 1.0mm for A, B, G, 0.2mm for C, D, E, 0.4mm for F. DISCUSSION With the description of three species of Stegophryxus, it now becomes possible to provide a generic description, thus: Female. Body longer than broad, bent to left so right side is longer; head roughly pyriform with subparallel sides, produced into point anteriorly, indented posterodorsally; first three pairs of oostegites arching far over head, others forming voluminous but tightly closed brood pouch; fifth oostegites much the largest, covering at least half of pereon ventrally and produced posteriorly into lateral sacs, that on right side extending slightly to greatly posteriorly. First five pereomeres bent around and enclosing head; sixth pereomere much the largest, concave both anteriorly and posteriorly. First two pereopods anterior to head, second two beside it; first five pereopods clustered forward, sharply reflexed, last two far back, more or less straight. Pleon of six pleomeres. First five pleomeres bearing biramous pleopods and lateral plates ranging from linear-lanceolate to subovate by species, all from common peduncle so pleopods

40 BULLETIX SOUTHERN CALIFORNIA ACADEMY OF SCIENCES VOLUM^ appear "triramous." Terminal pleomere with uniramous bulbous uropods, ranging, by species, from button-like structures to large clubs. Male. Body length about three times width, sides nearly parallel except for head and pleon. Head more than twice as wide as long, smoothly rounded anteriorly, usually set off from pereon, or at least lateral indentations indicating separation. All pereomeres separated by deep lateral incisions. Pleon from h h toms total body length, a single fused piece which is narrower than last pereomere, broadest behind anterior edge, rounded to pointed posteriorly. No pleonal appendages. Three other genera are closely related to Stegophryxus, their females being distinguishable from those of Stegophryxus by several characters. In Stegias Richardson, pereomere 5 is longest, the last oostegites are not produced into posterior sacs, the pleon is relatively much shorter and broader, and the fourth and fifth pleomeres lack lateral plates. There are no markedly elongate pereomeres in females of Anathelges Bonnier, the body is nearly as broad as long, and the brood pouch symmetrical. In females of Pseudostegias Shiino, the brood pouch does not extend beyond the head, and only the first four pleomeres bear lateral plates. The males of these four genera are more difficult to separate along generic lines. The distribution and host selection of the species of Stegophryxus are quite peculiar. First, this is evidently the only bopyrid genus found on both sides of the Americas and nowhere else. Stegophryxus hyptius, throughout its range, infests those species of Pagurus which occur on intertidal or shallow subtidal sandy bottoms, even though this range, in covering latitudes from about 26 N to 42 N, goes from an essentially tropical environment to nearly arctic environment. The distribution of S. hyphalus is completely different. It infests both known species of the pagurid genus Parapagurodes from a depth of 69 to 391m; and thus occurs nowhere close to the intertidal zone. Though the recorded latitudinal range of S. hyphalus is from 26 17'N to 36 27'N, there is little difference in temperature at the depths in question. The host and collection depth of S. thompsoni are unknown. In their description of this species, Nierstrasz and Brender a Brandis (1931) report: "Valparaiso. Kr0yer. Ein Weibchen mit Mannchen auf Pagurus sp." The label with the types bears the notation "af Pagurid," i.e., "from [a] pagurid," so the genus (and possibly even the family) of the host is uncertain. Janet Haig has kindly examined several pagurids and diogenids collected off Chile Peru and reports that none bore any abdomj parasites. As observed in a discussion of p, n 5 j thelges spp. (Markham, 1972), there seems to L little host specificity among athelgine bopy Therefore, it would be impossible to judge wh the host of the types of S. thompsoni might hav been even if more specimens should turn up ACKNOWLEDGMENTS Edward B. Hatfield collected and provided to me number of parasitized hermit crabs from the Mian, area. Richard W. Heard provided hermit crabs whk he and Charles Kellogg had collected in Geon and North Carolina, while the latter provided colle c. tion data from some of them. Torben Wolff allowed me to examine the types of 5. thompsoni. Janet Hai«examined hermit crabs from Chile and Peru in tfo Allan Hancock Foundation collections, furnished collection data on the hermit crabs from California and granted me permission to describe their parasites Patsy A. McLaughlin identified these crabs and made their parasites available to me as well as identifying many of the crabs collected along the Atlantic coast Thomas E. Bowman and Lowell P. Thomas critically reviewed the manuscript. This is publication No. 1734 of the Rosenstiel School of Marine and Atmospheric Science, University of Miami, and No. 1of the Arch Cape Marine Laboratory, Arch Cape. Oregon 97102. LITERATURE CITED Baffoni, G. M. 1953. Modificazione metaboliche dell' epatopancreas di "Callianassa laticauda" nella castrazione parassitaria. Atti Accad. Nai Lincei, 14:436-442. Bourdon, R. 1968. Les Bopyridae des mers Europeennes. Mem. Mus. Nat'l. Hist. Nat. (Paris), (n.s., A), 50(2):77-424. Caullery, M. 1950. Le parasitisme et la symbiose. Second Ed. C. Doin et Cie., Paris, 358 pp.. 1952. Parasitism and symbiosis. Sidgwicl and Jackson, London, xii + 340 pp. Florkin, M. 1960. Ecology and Metabolism. Pp- 395-410 in The Physiology of Crustacea. (T H. Waterman, ed.), Academic Press, New York. Vol. 1, xvii + 670 pp. Kaestner, A. 1967. Lehrbuch der speziellen Zoologie. Bd. I: Wirbellose, 2. Teil, Crustacea.

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